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. 2016 Feb 25;6(2):e008377. doi: 10.1136/bmjopen-2015-008377

Table 2.

Changes in outcome from trial entry to 18 months*

Biphasic (n=137) Aspart+detemir (n=138) Detemir (n=137) p Value biphasic vs aspart+detemir p Value biphasic vs detemir p Value aspart+detemir vs detemir
Carotid ultrasound measures
 Mean carotid IMT (mm)† −0.009 (−0.022 to 0.004) 0.000 (−0.013 to 0.013) −0.012 (−0.025 to 0.000) 0.2720 0.8173 0.1871
 Maximal carotid IMT (mm) −0.010 (−0.025 to 0.005) 0.001 (−0.014 to 0.016) −0.016 (−0.031 to −0.001) 0.2935 0.5734 0.1095
Body composition
 Weight (kg) 3.3 (2.7 to 4.0) 3.2 (2.6 to 3.9) 1.9 (1.3 to 2.6) 0.8102 0.0026 0.0055
 Body mass index (kg/m2) 1.1 (0.9 to 1.3) 1.0 (0.8 to 1.2) 0.6 (0.4 to 0.8) 0.7037 0.0021 0.0071
 Waist−hip ratio 0.00 (−0.01 to 0.01) 0.01 (0.00 to 0.02) 0.01 (0.00 to 0.02) 0.0926 0.0484 0.7516
Glycaemic control
 HbA1c (%) −1.00 (−1.16 to −0.83) −0.45 (−0.61 to −0.28) −0.26 (−0.43 to −0.09) <0.001 <0.001 0.1304
 HbA1c (mmol/mol) −10.9 (−12.7 to −9.1) −4.9 (−6.7 to −3.1) −2.8 (−4.7 to −1.0) <0.001 <0.001 0.1304
 HbA1c at 18 months (%) 7.78 (7.56 to 8.00) 8.19 (7.98 to 8.42) 8.42 (8.20 to 8.64) 0.0019 <0.001 0.1074
 HbA1c at 18 months (mmol/mol) 62 (59 to 64) 66 (64 to 69) 69 (66 to 71) 0.0019 <0.001 0.1074
 N (%) participants with HbA1c≤7.0% at end-of-trial 38 (28) 31 (22) 12 (9) 0.306 0.000 0.005
 Fasting p-glucose, mmol/L −2.0 (−2.6 to −1.4) −1.3 (−1.9 to −0.7) −2.4 (−3.1 to −1.8) 0.1108 0.3347 0.0109
 Fasting p-insulin (relative change from baseline) 0.92 (0.78 to 1.09) 0.57 (0.48 to 0.67) 0.52 (0.44 to 0.62) <0.001 <0.001 0.5103
 Fasting C peptide (relative change from baseline) 0.85 (0.76 to 0.94) 0.70 (0.63 to 0.78) 0.60 (0.54 to 0.67) 0.0110 <0.001 0.0480
 Insulin dose, end-of-trial (IU/kg/day) 0.96 (0.86 to 1.08) 1.15 (1.02 to 1.29) 1.58 (1.40 to 1.78) 0.0064 <0.001 <0.001
 Insulin dose, end-of-trial (IU/day) 95 (84 to 108) 116 (102 to 132) 158 (139 to 180) 0.080 <0.001 <0.001
 Insulin dose (relative change from baseline) 1.96 (1.82 to 2.11) 2.27 (2.10 to 2.45) 3.37 (3.11 to 3.65) 0.006 <0.001 <0.001
Blood pressure and lipids
 Systolic blood pressure (mm Hg) −6.7 (−9.4 to −3.9) −6.0 (−8.8 to −3.1) −3.5 (−6.4 to −0.6) 0.7282 0.1249 0.2391
 Diastolic blood pressure (mm Hg) −3.3 (−4.8 to −1.8) −2.9 (−4.4 to −1.4) −3.5 (−5.1 to −1.9) 0.6996 0.8795 0.5998
 Heart rate (bpm) −1.3 (−3.1 to 0.4) −0.5 (−2.3 to 1.2) −3.0 (−4.8 to −1.2) 0.5168 0.1853 0.0532
 Total cholesterol (mmol/L) 0.17 (0.03 to 0.31) 0.05 (−0.09 to 0.19) 0.19 (0.05 to 0.33) 0.2323 0.8254 0.1603
 LDL cholesterol (mmol/L) 0.15 (0.04 to 0.27) 0.06 (−0.06 to 0.18) 0.17 (0.05 to 0.29) 0.2634 0.9012 0.2187
 VLDL cholesterol (relative change from baseline) 0.96 (0.90 to 1.03) 1.02 (0.95 to 1.09) 1.01 (0.94 to 1.09) 0.2821 0.3111 0.9578
 HDL cholesterol (mmol/L) 0.03 (−0.00 to 0.07) −0.01 (−0.05 to 0.03) −0.01 (−0.05 to 0.02) 0.1112 0.0840 0.8722
 Triglycerides (relative change from baseline) 0.97 (0.91 to 1.05) 1.00 (0.93 to 1.08) 1.02 (0.95 to 1.10) 0.5826 0.3541 0.6989

The variables p-insulin, C peptide, insulin dose, VLDL cholesterol and triglycerides did not meet the criteria of a normal distribution and were accordingly log transformed. Therefore, these variables are presented in table 2 with relative change from baseline instead of absolute change.

To adjust for multiplicity, the significance level can be adjusted to 0.05/(K+1)/2 (where K represents the number of prespecified secondary outcomes) equalling, in this case, an α=0.0045.

*Intention-to-treat, mixed model analyses with random-effect person adjusted for stratification variables, results are presented as mean (95% CI).

†Between-group differences are analysed using multiple imputation of missing values.

HbA1c, glycated haemoglobin; HDL, high-density lipoprotein; IMT, intima-media thickness; LDL, low-density lipoprotein; VLDL, very low-density lipoprotein.